Laboratory of Molecular Immunogenetics, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, Maryland, USA.
Adv Exp Med Biol. 2011;716:123-42. doi: 10.1007/978-1-4419-9533-9_8.
Sphingosine-1-phosphate (S1P) plays important roles regulating functions of diverse biological systems, including the immune system. S1P affects immune cell function mostly by acting through its receptors at the cell membrane but it can also induce S1P receptor-independent responses in the cells where it is generated. S1P produced in allergically-stimulated mast cells mediates degranulation, cytokine and lipid mediator production and migration of mast cells towards antigen by mechanisms that are both S1P receptor-dependent and independent. Even in the absence of an antigen challenge, the differentiation and responsiveness of mast cells can be affected by chronic exposure to elevated S1P from a nonmast cell source, whichmay occur under pathophysiological conditions, potentially leading to the hyper-responsiveness of mast cells. The role of S1P extends beyond the regulation of the function of mast cells to the regulation of the surrounding or distal environment. S1P is exported out of antigen-stimulated mast cells and into the extracellular space and the resulting S1P gradient within the tissue may influence diverse surrounding tissue cells and several aspects of the allergic disease, such as inflammation or tissue remodeling. Furthermore, recent findings indicate that vasoactive mediators released systemically by mast cells induce the production of S1P in nonhematopoietic compartments, where it plays a role in regulating the vascular tone and reducing the hypotension characteristic of the anaphy lactic shock and thus helping the recovery. The dual actions of S1P, promoting the immediate response of mast cells, while controlling the systemic consequences of mast cell activity will be discussed in detail.
鞘氨醇-1-磷酸(S1P)在调节多种生物系统的功能方面发挥着重要作用,包括免疫系统。S1P 主要通过作用于细胞膜上的受体来影响免疫细胞的功能,但它也可以在产生 S1P 的细胞中诱导非 S1P 受体依赖性反应。在过敏刺激的肥大细胞中产生的 S1P 通过依赖和不依赖 S1P 受体的机制介导脱颗粒、细胞因子和脂质介质的产生以及肥大细胞向抗原的迁移。即使没有抗原挑战,肥大细胞的分化和反应性也可能受到来自非肥大细胞来源的升高的 S1P 的慢性暴露的影响,这种情况可能发生在病理生理条件下,潜在地导致肥大细胞的高反应性。S1P 的作用不仅限于调节肥大细胞的功能,还涉及调节周围或远处的环境。S1P 从抗原刺激的肥大细胞中输出到细胞外空间,组织内的 S1P 梯度可能影响周围的多种组织细胞,并影响过敏疾病的几个方面,如炎症或组织重塑。此外,最近的研究结果表明,肥大细胞系统性释放的血管活性介质诱导非造血区室中 S1P 的产生,在非造血区室中 S1P 发挥调节血管张力和降低过敏性休克特征性低血压的作用,从而有助于恢复。S1P 的双重作用,促进肥大细胞的即刻反应,同时控制肥大细胞活性的全身后果,将在本文中详细讨论。